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Ds Anterior, Ds Base, Ds Head-Neck, Ds Head, Flex (s +2 more)

FDA 510(k)

Class II (US FDA 510(k))

510(k) K123492

by Philips Medical Systems

Identifiers

510(k) Number
K123492 FDA 510(k)
FDA Product Code
MOS FDA 510(k)
Models / Variants
s FDA 510(k)
M FDA 510(k)
L FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 892.1000 FDA 510(k)
Regulation Number
892.1000 FDA 510(k)
Advisory Committee
Radiology FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Ds Anterior, Ds Base, Ds Head-Neck, Ds Head, Flex (s +2 more) by Philips Medical Systems — Class II — FDA_510K — listed in FDA 510(k) — 3 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Philips Medical Systems

Sources (1)

  • FDA 510(k) K123492 24 fields · synced Jun 18, 2026